Ballard D W, Voss E W
Mol Immunol. 1982 Jun;19(6):793-9. doi: 10.1016/0161-5890(82)90005-0.
The NZB/NZW F1 murine model for the autoimmune disease systemic lupus erythematosus (SLE) has been employed in somatic cell hybridizations to develop hybridoma autoantibodies with double-stranded (ds) DNA specificity. Monoclonal anti-DNA antibodies from one hybridoma cell line were purified and analysed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and isoelectric focusing. Results of comparative binding studies with tritiated [3H]-colicin E1 plasmid DNA probes suggested preferential binding for the native DNA conformation relative to single-stranded DNA. [3H]dsDNA binding was inhibited by several ribohomopolymers (poly G, U and I) but not by free nucleotides, indicating that the phosphodiester-ribose backbone may contribute to the binding specificity of the clonotype.
用于自身免疫性疾病系统性红斑狼疮(SLE)的NZB/NZW F1小鼠模型已被用于体细胞杂交,以开发具有双链(ds)DNA特异性的杂交瘤自身抗体。从一个杂交瘤细胞系中纯化出单克隆抗DNA抗体,并通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和等电聚焦进行分析。用氚标记的[3H] - 大肠杆菌素E1质粒DNA探针进行的比较结合研究结果表明,相对于单链DNA,该抗体对天然DNA构象具有优先结合性。几种核糖同聚物(聚G、U和I)可抑制[3H]dsDNA结合,但游离核苷酸则不能,这表明磷酸二酯 - 核糖主链可能有助于该克隆型的结合特异性。